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吉西他滨联合表柔比星治疗铂耐药或难治性晚期卵巢癌的Ⅰ期研究。

A phase I study of gemcitabine and epirubicin for the treatment of platinum-resistant or refractory advanced ovarian cancer.

作者信息

Pignata S, Varriale E, Casella G, Iodice F, De Placido G, Perrone F, Tramontana F, Ricchi P, De Vivo R, Costanzo R, Vernaglia A, Tramontana S

机构信息

Divisione di Oncologia Medica B, Istituto Nazionale Tumori, Napoli, Italy.

出版信息

Ann Oncol. 2000 May;11(5):613-6. doi: 10.1023/a:1008344528791.

Abstract

BACKGROUND

Gemcitabine is active in patients with otherwise resistant or refractory ovarian cancer. As the drug is well tolerated, studies using gemcitabine combined with other antineoplastic agents are needed. The aim of the study was to determine the maximum tolerated dose (MTD) of epirubicin combined with gemcitabine, with and without support of G-CSF.

PATIENTS AND METHODS

Patients with platinum-resistant or refractory ovarian cancer were eligible. Gemcitabine (G) (starting dose 800 mg/m2 day 1 and 8; 200 mg/m2 escalation per level) and epirubicin (E) (starting dose 60 mg/m2 day 1; 15 mg/m2 escalation per level) were given every 21 days for four to six cycles. G-CSF (filgrastim 5 microg/kg/die) was given in case of grade 4 neutropenia (levels without support) or from day 9 up to leukocyte count > 10.000/mm3 after nadir (levels with support). Cohorts of three patients were enrolled at each level, and another three patients were planned, if one dose-limiting toxicity (DLT) was registered. MTD was determined first without and then with G-CSF.

RESULTS

Four levels were studied (G 800 + E 60; G 1000 + E 60; G 1000 + E 75; G 1000 + E 75 + G-CSF) with four, four, three and three patients enrolled, respectively. DLT (grade 4 febrile neutropenia) was observed in two patients at level 3. Thus, G1000 + E 60 mg/m2 was the MTD without G-CSF. The addition of prophylactic G-CSF did not allow a further increase of the dose and grade 4 thrombocytopenia was the DLT at level 4. Non-hematological toxicity was mild. Grade 2 mucositis was reported in four patients. Among the 13 patients with measurable or evaluable disease, 3 partial responses were observed for an overall response rate of 23.1%.

CONCLUSIONS

The combination of gemcitabine 1000 mg/m2 (day 1, 8) and epirubicin at 60 mg/m2 (day 1) is a feasible therapy. Grade 4 neutropenia is frequent and G-CSF support is often required. With prophylactic support of G-CSF, the DLT is thrombocytopenia.

摘要

背景

吉西他滨对其他治疗耐药或难治的卵巢癌患者有活性。由于该药物耐受性良好,需要开展吉西他滨与其他抗肿瘤药物联合应用的研究。本研究的目的是确定表柔比星联合吉西他滨在有或无粒细胞集落刺激因子(G-CSF)支持情况下的最大耐受剂量(MTD)。

患者与方法

符合条件的患者为铂类耐药或难治的卵巢癌患者。吉西他滨(G)(起始剂量800mg/m²,第1天和第8天给药;每级剂量递增200mg/m²)和表柔比星(E)(起始剂量60mg/m²,第1天给药;每级剂量递增15mg/m²)每21天给药一次,共进行4至6个周期。若出现4级中性粒细胞减少(无支持情况下的水平),或在最低点后第9天直至白细胞计数>10000/mm³(有支持情况下的水平)时,给予G-CSF(非格司亭5μg/kg/天)。每个剂量水平入组3例患者,若出现1例剂量限制性毒性(DLT),则计划再入组3例患者。首先在无G-CSF支持的情况下确定MTD,然后在有G-CSF支持的情况下确定MTD。

结果

研究了4个剂量水平(G 800 + E 60;G 1000 + E 60;G 1000 + E 75;G 1000 + E 75 + G-CSF),分别入组4例、4例、3例和3例患者。在第3个剂量水平有2例患者出现DLT(4级发热性中性粒细胞减少)。因此,G1000 + E 60mg/m²是无G-CSF支持情况下的MTD。预防性添加G-CSF未能进一步提高剂量,4级血小板减少是第4个剂量水平的DLT。非血液学毒性较轻。4例患者报告有2级黏膜炎。在13例有可测量或可评估疾病的患者中,观察到3例部分缓解,总缓解率为23.1%。

结论

吉西他滨1000mg/m²(第1天、第8天)与表柔比星60mg/m²(第1天)联合应用是一种可行的治疗方法。4级中性粒细胞减少很常见,常需要G-CSF支持。在G-CSF预防性支持下,DLT为血小板减少。

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